By replacing the defective gene associated with Dravet syndrome in mice, scientists successfully alleviated symptoms without side effects.

In a groundbreaking advancement for families grappling with the challenges of Dravet syndrome, a rare and life-altering form ...

Scientists developed a promising gene replacement therapy for Dravet syndrome in mice. The therapy alleviated symptoms ...

Snakes are one of the most dangerous yet fascinating reptiles. With their stunning patterns, slithering noises and poisonous ...

LncRNAs and circRNAs are key regulators of gene expression, influencing disease mechanisms and offering potential as ...

Rua Dr. Diogo de Faria, 1087 – 9º andar – Vila Clementino 04037-003 São Paulo/SP - Brasil E-mail: [email protected] ...

Mammalian genomes are organized by multi-level folding, yet how this organization contributes to cell type-specific transcription remain unclear. We uncovered that the nuclear protein SATB1 ...

A small team of computational and evolutionary biologists from the University of Chinese Academy of Sciences, Zhongshan ...

Emeritus Professor of Experimental Haematology, Constanze Bonifer, wins prestigious award for advancing her field of research.

Dec. 10, 2024 — In a single IV injection, a gene therapy targeting cBIN1 can reverse the effects of heart failure and restore heart function in a large animal model. The therapy increases the ...

CRISPR is a gene editing tool that allows scientists to precisely alter ... The researchers found that about 9% of the ...

Researchers used powerful tech to analyse thousands of individual cells at once, considering which genes are active and how DNA is organised within each cell.